drugset / Trial / NCT00637949

Safety of Lumiracoxib in Patients With Osteoarthritis

NCT00637949

Phase 3 Completed 309 enrolled Novartis
RandomizedParallel-groupDouble-blindTreatment

Summary

This safety study evaluated the incidence of gastrointestinal adverse events and edema in patients with osteoarthritis treated with lumiracoxib and rofecoxib as comparator

Timeline

Start
2000-12
Primary completion
2001-03
Completion
2001-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator rofecoxib Small molecule 25 mg Oral

Indications